Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8042149
RORA
0.882 0.160 15 60832754 intron variant T/G snv 0.44 3
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs1042357
ALOX12 ; ALOX12-AS1
0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 2
rs4775301
RORA
0.925 0.040 15 60834660 intron variant T/C;G snv 2
rs363276
SLC18A2
1.000 0.040 10 117274298 intron variant T/C;G snv 1
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs4311
ACE
0.882 0.200 17 63483402 intron variant T/C snv 0.60 3
rs56242606
VWDE
1.000 0.040 7 12382283 intron variant T/C snv 5.3E-02 2
rs1187327
NTRK2
1.000 0.040 9 84673625 intron variant T/C snv 0.50 1
rs12458282
MBP
1.000 0.040 18 77061897 intron variant T/C snv 0.24 1
rs2108977
TPH1
1.000 0.040 11 18019049 3 prime UTR variant T/C snv 0.47 1
rs28932171
ANK3
1.000 0.040 10 60071532 missense variant T/C snv 7.2E-02 7.3E-02 1
rs356195
SNCA
1.000 0.040 4 89762017 intron variant T/C snv 0.81 1
rs58649573
LHX2
1.000 0.040 9 124005148 intron variant T/C snv 1
rs682457 1.000 0.040 11 88216364 intergenic variant T/C snv 0.14 1
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs406001 1.000 0.040 7 51938719 intergenic variant T/A;C snv 1
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 9
rs8041061
RORA
0.925 0.040 15 60832639 intron variant G/T snv 0.39 2